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DOI 10.1111/apm.12586

Медицинская библиотека · APMIS : acta pathologica, microbiologica, et immunologica Scandinavica · 2016

Histopathological changes in skeletal muscle associated with chronic ischaemia.

Roos Sara, Fyhr Ing-Marie, Sunnerhagen Katharina S, Moslemi Ali-Reza, Oldfors Anders, Ullman Michael

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Аннотация

Muscle biopsy is an essential part in the diagnostic workup in patients with suspected neuromuscular disorders. It is therefore important to be aware of morphological alterations that can be caused by systemic factors or natural ageing. Chronic limb ischaemia is frequent in elderly individuals. This study was performed to examine histopathological and mitochondrial changes in muscle in patients with chronic critical limb ischaemia. Muscle biopsy of skeletal muscle of the lower limb of patients with chronic ischaemia leading to amputation was performed and compared with muscle biopsies of healthy, age-matched controls. The histopathological abnormalities included fibrosis, necrosis, atrophy, glycogen depletion, internal nuclei, rimmed vacuoles, fibre type grouping, cytochrome c oxidase deficient fibres, MHC-I upregulation, and signs of microangiopathy. The only alteration found in age-matched controls was a few cytochrome c oxidase deficient fibres. There were also increased levels of multiple mitochondrial DNA deletions in ischaemic muscles compared with controls. Critical limb ischaemia is associated with significant histopathological changes in muscle tissue and also increased levels of mitochondrial DNA deletions. Since the alterations mimic different primary myopathic changes, chronic ischaemia is important to consider as a differential diagnosis in elderly individuals, investigated with muscle biopsy for muscle disease.

Для цитирования: Roos Sara, Fyhr Ing-Marie, Sunnerhagen Katharina S, Moslemi Ali-Reza, Oldfors Anders, Ullman Michael. Histopathological changes in skeletal muscle associated with chronic ischaemia.. APMIS : acta pathologica, microbiologica, et immunologica Scandinavica. 2016. DOI: 10.1111/apm.12586.

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